Medical Device Recalls
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1 result found
510(K) Number: K034055 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IMMULITE® 2500 CK-MB L5KCP --- Catalog number: L5KCP2 (200 tests), L5KCP6 (600 tests) --- Test code:... | 2 | 03/21/2012 |
FEI # 2432235 Siemens Healthcare Diagnostics |
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